Sobre este puesto de Director of Projects, Clinical Assessment Training and Surveillance (CATS) - Europe - Remote en Worldwide Clinical Trials
Who we are
We’re a global, midsize CRO that pushes boundaries, innovates and invents because the path to a cure for the world’s most persistent diseases is not paved by those who play it safe. It is built by those who take pioneering, creative approaches and implement them with quality and excellence.
We are Worldwide Clinical Trials, and we are a global team of over 3,500+ experts, bright thinkers, dreamers and doers and, together, we are changing the way the world experiences CROs – in the best possible way.
Our mission is to work with passion and purpose every day to improve lives and we are looking for others who value this same pursuit.
Why Worldwide
We believe everyone plays an important role in making a world of difference for patients and their caregivers. From our hands-on, accessible leaders, to our cohesive and supportive teams, we are committed to enabling professionals from all backgrounds and experiences to succeed. We prioritize cultivating a diverse and inclusive environment that continues to promote collaboration and creativity. We are proud to be a workplace where people thrive by being themselves and are inspired to do their best work every day. Join us!
What the Clinical Assessment Training and Surveillance Department does at Worldwide
Clinical Assessment Technologies (CAT) is a team of highly experienced clinicians and operations experts whose purpose is to improve clinical outcomes data by reducing data variability associated with lack of training, inconsistent approaches to scale administration and scoring, placebo response, and incorrect source. The members of CAT have extensive industry-related experience stemming from their time working on the site level for sponsors and other service providers. Additionally, the CAT team has conducted more than 75 international Phase I to Phase IV trials and has trained over 7,000 raters.
What you will do
Engages with senior management to establish strategic department initiatives and objectives
Drive new QMD developments, including authoring and reviewing QMD documents and guidance documents
Active participant in the identification and development of new service arms, Active participant in the improvement of existing service arms
Drive business development activities for CAT, including proposals input, participation in capabilities and bid defense activities
Identify clinical needs for upcoming and current projects, track and review with CAT Clinical Staff and CAT Leadership
Accountable for the development of assessment training content and plans by ensuring the training curriculum and materials (including training videos) meet protocol, copyright holder, author, and sponsor requirements
What you will bring to the role
Strong organizational skills, detail- and service-oriented, with excellent management skills
Strong understanding of best business practices with respect to rater training, methodologies, and corporate discipline
Personality focused on meeting timelines consistently and being able to effectively work under pressure
Excels in writing and verbal communication skills in order to clearly and concisely present information
Ability to handle multiple tasks and many administrative details in a fast-paced and constantly changing environment
Clear ability to proactively identify and escalate potential project issues to appropriate CAT and Worldwide staff
Strong proficiency in all MS-Office applications including Microsoft Word, Excel, Teams, and PowerPoint
Your experience
Minimum of earned Master’s Degree in life sciences or equivalent
At least 10 years clinical trial experience with clinical assessments, independently organizing and conducting projects, and presenting at Investigators’ Meetings or similar presentations as expert clinicians
Preferred at least 4 years of experience managing team members or providing direct clinical mentorship
Strong applied knowledge of pivotal efficacy measure administration conventions that can be used in the administration and review of such instruments and communicated to train assessors
Knowledge of operational aspects regarding Phase I-IV clinical research trials and experience working with a Contract Research Organization/Rater Training Organization
Excellent collaborative skills and ability to work cross-functionally to drive projects and initiatives
Strong ability to apply knowledge and utilize available resources to develop new ideas and improve existing processes
Excellent knowledge of SOPs, ICH/GCP/regulatory guidelines
Competent working with data and numbers
Willingness to travel
We love knowing that someone is going to have a better life because of the work we do.
To view our other roles, check out our careers page at Discover a world of difference at Worldwide! For more information on Worldwide, visit www.Worldwide.com or connect with us on LinkedIn.
Worldwide is an equal opportunity employer that is committed to enabling professionals from all backgrounds and experiences to succeed and, to that end, we prioritize attracting diverse talent and cultivating an inclusive environment that encourages collaboration and creativity. We know that when our employees feel appreciated and included, they can be more creative, innovative, and successful. We’re on a mission to hire the very best and are committed to creating exceptional employee experiences where everyone is respected and has access to equal opportunity. We provide equal employment opportunities to all employees and applicants regardless of race, color, ethnicity, ancestry, religion, national origin, gender, sex, gender identity or expression, sexual orientation, age, citizenship, marital or parental status, disability, military status, or other class protected by applicable law.